rs281865069

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs281865069(C;G)

Make rs281865069(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154571724

Gene

CHRNB2

is a	snp
is	mentioned by
dbSNP	rs281865069
dbSNP (classic)	rs281865069
ClinGen	rs281865069
ebi	rs281865069
HLI	rs281865069
Exac	rs281865069
Gnomad	rs281865069
Varsome	rs281865069
LitVar	rs281865069
Map	rs281865069
PheGenI	rs281865069
Biobank	rs281865069
1000 genomes	rs281865069
hgdp	rs281865069
ensembl	rs281865069
geneview	rs281865069
scholar	rs281865069
google	rs281865069
pharmgkb	rs281865069
gwascentral	rs281865069
openSNP	rs281865069
23andMe	rs281865069
SNPshot	rs281865069
SNPdbe	rs281865069
MSV3d	rs281865069
GWAS Ctlg	rs281865069

Max Magnitude

0

ClinVar
Risk	rs281865069(G;G)
Alt	rs281865069(G;G)
Reference	Rs281865069(C;C)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	CHRNB2
CLNDBN	Epilepsy, nocturnal frontal lobe, type 3
Reversed	0
HGVS	NC_000001.10:g.154544200C>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033931.2,